Myotonia (MYT)
Gene or Region: CLCN1
Reference Variant: A
Mutant Variant: C
Affected Breeds: New Forest Pony
Research Confidence: Moderate - Mutation was not found in 56 control horse of 13 different breeds, and mutations in the same gene result in myotonia in other species
Explanation of Results: MYT/MYT = homozygous for Myotonia, trait expressed MYT/n = heterozygous for Myotonia, carrier n/n = no variant detected
General Description
Myotonia is a rare disorder involving a slowed relaxation of muscles after contraction. The most well-known example of myotonia is “fainting goats,” a breed that is characterized by sudden rigidy and/or falling over when startled. In the single documented horse, this resulted in a protruding third eyelid when excited, as well as problems with muscle stiffness (and thus difficulty in rising and movement). This mutation is believed to be a more recent occurrence within the New Forest Pony breed.
Gene Information _CLCN1 _is a voltage-dependent chloride channel involved in signaling in muscles. Mutations in this gene have been associated with myotonia is humans, dogs, and goats. This specific mutation described in the horse results in an amino acid change, which likely alters the function of the encoded protein.
References
Wijnberg ID et al., “A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony.” (2012) Neuromuscul Disord. 22: 361-7. PMID: 22197188
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